US10280380B2 - Composition of additives and high-performance fuel comprising such a composition - Google Patents

Composition of additives and high-performance fuel comprising such a composition Download PDF

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US10280380B2
US10280380B2 US15/119,807 US201515119807A US10280380B2 US 10280380 B2 US10280380 B2 US 10280380B2 US 201515119807 A US201515119807 A US 201515119807A US 10280380 B2 US10280380 B2 US 10280380B2
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carbon atoms
additive
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diesel
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US20170058225A1 (en
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Géraldine Papin
Julien GUEIT
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TotalEnergies Marketing Services SA
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Total Marketing Services SA
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    • C—CHEMISTRY; METALLURGY
    • C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10L—FUELS NOT OTHERWISE PROVIDED FOR; NATURAL GAS; SYNTHETIC NATURAL GAS OBTAINED BY PROCESSES NOT COVERED BY SUBCLASSES C10G, C10K; LIQUEFIED PETROLEUM GAS; ADDING MATERIALS TO FUELS OR FIRES TO REDUCE SMOKE OR UNDESIRABLE DEPOSITS OR TO FACILITATE SOOT REMOVAL; FIRELIGHTERS
    • C10L10/00—Use of additives to fuels or fires for particular purposes
    • C10L10/04—Use of additives to fuels or fires for particular purposes for minimising corrosion or incrustation
    • C—CHEMISTRY; METALLURGY
    • C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10L—FUELS NOT OTHERWISE PROVIDED FOR; NATURAL GAS; SYNTHETIC NATURAL GAS OBTAINED BY PROCESSES NOT COVERED BY SUBCLASSES C10G, C10K; LIQUEFIED PETROLEUM GAS; ADDING MATERIALS TO FUELS OR FIRES TO REDUCE SMOKE OR UNDESIRABLE DEPOSITS OR TO FACILITATE SOOT REMOVAL; FIRELIGHTERS
    • C10L1/00—Liquid carbonaceous fuels
    • C10L1/10—Liquid carbonaceous fuels containing additives
    • C10L1/14—Organic compounds
    • C10L1/18—Organic compounds containing oxygen
    • C—CHEMISTRY; METALLURGY
    • C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10L—FUELS NOT OTHERWISE PROVIDED FOR; NATURAL GAS; SYNTHETIC NATURAL GAS OBTAINED BY PROCESSES NOT COVERED BY SUBCLASSES C10G, C10K; LIQUEFIED PETROLEUM GAS; ADDING MATERIALS TO FUELS OR FIRES TO REDUCE SMOKE OR UNDESIRABLE DEPOSITS OR TO FACILITATE SOOT REMOVAL; FIRELIGHTERS
    • C10L1/00—Liquid carbonaceous fuels
    • C10L1/10—Liquid carbonaceous fuels containing additives
    • C10L1/14—Organic compounds
    • C10L1/22—Organic compounds containing nitrogen
    • C—CHEMISTRY; METALLURGY
    • C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10L—FUELS NOT OTHERWISE PROVIDED FOR; NATURAL GAS; SYNTHETIC NATURAL GAS OBTAINED BY PROCESSES NOT COVERED BY SUBCLASSES C10G, C10K; LIQUEFIED PETROLEUM GAS; ADDING MATERIALS TO FUELS OR FIRES TO REDUCE SMOKE OR UNDESIRABLE DEPOSITS OR TO FACILITATE SOOT REMOVAL; FIRELIGHTERS
    • C10L10/00—Use of additives to fuels or fires for particular purposes
    • C10L10/06—Use of additives to fuels or fires for particular purposes for facilitating soot removal
    • C—CHEMISTRY; METALLURGY
    • C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10L—FUELS NOT OTHERWISE PROVIDED FOR; NATURAL GAS; SYNTHETIC NATURAL GAS OBTAINED BY PROCESSES NOT COVERED BY SUBCLASSES C10G, C10K; LIQUEFIED PETROLEUM GAS; ADDING MATERIALS TO FUELS OR FIRES TO REDUCE SMOKE OR UNDESIRABLE DEPOSITS OR TO FACILITATE SOOT REMOVAL; FIRELIGHTERS
    • C10L1/00—Liquid carbonaceous fuels
    • C10L1/10—Liquid carbonaceous fuels containing additives
    • C10L1/14—Organic compounds
    • C10L1/18—Organic compounds containing oxygen
    • C10L1/19—Esters ester radical containing compounds; ester ethers; carbonic acid esters
    • C10L1/191—Esters ester radical containing compounds; ester ethers; carbonic acid esters of di- or polyhydroxyalcohols
    • C—CHEMISTRY; METALLURGY
    • C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10L—FUELS NOT OTHERWISE PROVIDED FOR; NATURAL GAS; SYNTHETIC NATURAL GAS OBTAINED BY PROCESSES NOT COVERED BY SUBCLASSES C10G, C10K; LIQUEFIED PETROLEUM GAS; ADDING MATERIALS TO FUELS OR FIRES TO REDUCE SMOKE OR UNDESIRABLE DEPOSITS OR TO FACILITATE SOOT REMOVAL; FIRELIGHTERS
    • C10L1/00—Liquid carbonaceous fuels
    • C10L1/10—Liquid carbonaceous fuels containing additives
    • C10L1/14—Organic compounds
    • C10L1/22—Organic compounds containing nitrogen
    • C10L1/221—Organic compounds containing nitrogen compounds of uncertain formula; reaction products where mixtures of compounds are obtained
    • C—CHEMISTRY; METALLURGY
    • C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10L—FUELS NOT OTHERWISE PROVIDED FOR; NATURAL GAS; SYNTHETIC NATURAL GAS OBTAINED BY PROCESSES NOT COVERED BY SUBCLASSES C10G, C10K; LIQUEFIED PETROLEUM GAS; ADDING MATERIALS TO FUELS OR FIRES TO REDUCE SMOKE OR UNDESIRABLE DEPOSITS OR TO FACILITATE SOOT REMOVAL; FIRELIGHTERS
    • C10L1/00—Liquid carbonaceous fuels
    • C10L1/10—Liquid carbonaceous fuels containing additives
    • C10L1/14—Organic compounds
    • C10L1/22—Organic compounds containing nitrogen
    • C10L1/222—Organic compounds containing nitrogen containing at least one carbon-to-nitrogen single bond
    • C10L1/2222—(cyclo)aliphatic amines; polyamines (no macromolecular substituent 30C); quaternair ammonium compounds; carbamates
    • C—CHEMISTRY; METALLURGY
    • C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10L—FUELS NOT OTHERWISE PROVIDED FOR; NATURAL GAS; SYNTHETIC NATURAL GAS OBTAINED BY PROCESSES NOT COVERED BY SUBCLASSES C10G, C10K; LIQUEFIED PETROLEUM GAS; ADDING MATERIALS TO FUELS OR FIRES TO REDUCE SMOKE OR UNDESIRABLE DEPOSITS OR TO FACILITATE SOOT REMOVAL; FIRELIGHTERS
    • C10L1/00—Liquid carbonaceous fuels
    • C10L1/10—Liquid carbonaceous fuels containing additives
    • C10L1/14—Organic compounds
    • C10L1/22—Organic compounds containing nitrogen
    • C10L1/232—Organic compounds containing nitrogen containing nitrogen in a heterocyclic ring
    • C—CHEMISTRY; METALLURGY
    • C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10L—FUELS NOT OTHERWISE PROVIDED FOR; NATURAL GAS; SYNTHETIC NATURAL GAS OBTAINED BY PROCESSES NOT COVERED BY SUBCLASSES C10G, C10K; LIQUEFIED PETROLEUM GAS; ADDING MATERIALS TO FUELS OR FIRES TO REDUCE SMOKE OR UNDESIRABLE DEPOSITS OR TO FACILITATE SOOT REMOVAL; FIRELIGHTERS
    • C10L1/00—Liquid carbonaceous fuels
    • C10L1/10—Liquid carbonaceous fuels containing additives
    • C10L1/14—Organic compounds
    • C10L1/22—Organic compounds containing nitrogen
    • C10L1/234—Macromolecular compounds
    • C10L1/238—Macromolecular compounds obtained otherwise than by reactions involving only carbon-to-carbon unsaturated bonds
    • C10L1/2383—Polyamines or polyimines, or derivatives thereof (poly)amines and imines; derivatives thereof (substituted by a macromolecular group containing 30C)
    • C—CHEMISTRY; METALLURGY
    • C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10L—FUELS NOT OTHERWISE PROVIDED FOR; NATURAL GAS; SYNTHETIC NATURAL GAS OBTAINED BY PROCESSES NOT COVERED BY SUBCLASSES C10G, C10K; LIQUEFIED PETROLEUM GAS; ADDING MATERIALS TO FUELS OR FIRES TO REDUCE SMOKE OR UNDESIRABLE DEPOSITS OR TO FACILITATE SOOT REMOVAL; FIRELIGHTERS
    • C10L2200/00—Components of fuel compositions
    • C10L2200/04—Organic compounds
    • C10L2200/0407—Specifically defined hydrocarbon fractions as obtained from, e.g. a distillation column
    • C10L2200/0438—Middle or heavy distillates, heating oil, gasoil, marine fuels, residua
    • C10L2200/0446—Diesel
    • C—CHEMISTRY; METALLURGY
    • C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10L—FUELS NOT OTHERWISE PROVIDED FOR; NATURAL GAS; SYNTHETIC NATURAL GAS OBTAINED BY PROCESSES NOT COVERED BY SUBCLASSES C10G, C10K; LIQUEFIED PETROLEUM GAS; ADDING MATERIALS TO FUELS OR FIRES TO REDUCE SMOKE OR UNDESIRABLE DEPOSITS OR TO FACILITATE SOOT REMOVAL; FIRELIGHTERS
    • C10L2200/00—Components of fuel compositions
    • C10L2200/04—Organic compounds
    • C10L2200/0461—Fractions defined by their origin
    • C10L2200/0469—Renewables or materials of biological origin
    • C10L2200/0476—Biodiesel, i.e. defined lower alkyl esters of fatty acids first generation biodiesel
    • C—CHEMISTRY; METALLURGY
    • C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10L—FUELS NOT OTHERWISE PROVIDED FOR; NATURAL GAS; SYNTHETIC NATURAL GAS OBTAINED BY PROCESSES NOT COVERED BY SUBCLASSES C10G, C10K; LIQUEFIED PETROLEUM GAS; ADDING MATERIALS TO FUELS OR FIRES TO REDUCE SMOKE OR UNDESIRABLE DEPOSITS OR TO FACILITATE SOOT REMOVAL; FIRELIGHTERS
    • C10L2230/00—Function and purpose of a components of a fuel or the composition as a whole
    • C10L2230/22—Function and purpose of a components of a fuel or the composition as a whole for improving fuel economy or fuel efficiency
    • C—CHEMISTRY; METALLURGY
    • C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10L—FUELS NOT OTHERWISE PROVIDED FOR; NATURAL GAS; SYNTHETIC NATURAL GAS OBTAINED BY PROCESSES NOT COVERED BY SUBCLASSES C10G, C10K; LIQUEFIED PETROLEUM GAS; ADDING MATERIALS TO FUELS OR FIRES TO REDUCE SMOKE OR UNDESIRABLE DEPOSITS OR TO FACILITATE SOOT REMOVAL; FIRELIGHTERS
    • C10L2270/00—Specifically adapted fuels
    • C10L2270/02—Specifically adapted fuels for internal combustion engines
    • C10L2270/026—Specifically adapted fuels for internal combustion engines for diesel engines, e.g. automobiles, stationary, marine
    • C—CHEMISTRY; METALLURGY
    • C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10L—FUELS NOT OTHERWISE PROVIDED FOR; NATURAL GAS; SYNTHETIC NATURAL GAS OBTAINED BY PROCESSES NOT COVERED BY SUBCLASSES C10G, C10K; LIQUEFIED PETROLEUM GAS; ADDING MATERIALS TO FUELS OR FIRES TO REDUCE SMOKE OR UNDESIRABLE DEPOSITS OR TO FACILITATE SOOT REMOVAL; FIRELIGHTERS
    • C10L2300/00—Mixture of two or more additives covered by the same group of C10L1/00 - C10L1/308
    • C10L2300/20—Mixture of two components
    • Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y02—TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
    • Y02E—REDUCTION OF GREENHOUSE GAS [GHG] EMISSIONS, RELATED TO ENERGY GENERATION, TRANSMISSION OR DISTRIBUTION
    • Y02E50/00—Technologies for the production of fuel of non-fossil origin
    • Y02E50/10—Biofuels, e.g. bio-diesel
    • Y02E50/13—

Definitions

  • the present invention relates to compositions of additives and fuels containing such compositions of additives.
  • the present invention relates in particular to compositions of additives for diesel and/or bio diesel fuel.
  • the present invention further relates to the use of such fuels in diesel engines to improve their performance, in particular in diesel engines with a fuel injection system of type Euro 3 to Euro 6.
  • Fuels that are marketed must comply with national or supranational specifications (for example standard EN 590 for diesel fuels in the EU). For commercial fuels, there is no legal obligation concerning the incorporation of additives. From the commercial point of view, in the area of fuel distribution, a distinction is made between “base price” fuels, with few or no additives, and higher-grade fuels in which one or more additives are incorporated to improve their performance (beyond the regulatory performance).
  • the phenomenon of lacquering does not relate to the deposits that are present outside the injection system 5 or 5 ′ ( FIGS. 1 and 3 ) and are associated with coking, which is the cause of fouling and partial or complete clogging of the injection nozzles 4 or 4 ′ (nozzle “coking” or “fouling”). Lacquering and coking are two quite distinct phenomena both with respect to the causes of these deposits, the conditions of appearance of these deposits and the place where these deposits occur. Coking is a phenomenon that only appears downstream of a diesel injection system.
  • the deposits 5 ′ formed are characterized in that they result from pyrolysis of the hydrocarbons entering the combustion chamber and have the appearance of carbonaceous deposits.
  • the tendency to coking is far less pronounced. This coking is simulated conventionally by the standard engine test CEC F098-08 DW10B, especially when the fuel tested is contaminated with metallic zinc.
  • the injectors 3 of direct-injection diesel engines comprise a needle 2 , the lift of which allows precise control of the quantity of fuel injected at high pressure directly into the combustion chamber. Lacquering causes the appearance of deposits 1 , which appear specifically at the level of the needles 2 of the injectors 3 ( FIGS. 1 and 2 ). The phenomenon of lacquering is associated with the formation of soap and/or lacquer in the internal components of the injection systems of engines for fuels of the diesel and/or bio diesel type.
  • the lacquering deposit 1 may be located on the end 4 of the needles 2 of injectors 3 , both on the head and on the body of the needles 2 of the fuel injection system but also throughout the whole system for controlling needle lift (valves not shown) of the injection system. This phenomenon is particularly marked for engines using higher-grade diesel fuels. When these deposits are present in large quantities, the mobility of the needle 2 of the injector 3 fouled by these deposits 1 is compromised. Moreover, in contrast to coking, lacquering may also cause an increase in engine noise and sometimes problems when starting. In fact, the parts of the needles 2 fouled by the deposits of soap and/or of lacquer 1 may stick to the inside walls of the injector 3 . The needles 2 are then blocked and the fuel no longer passes through.
  • these salts are insoluble in low-sulphur diesel fuels and, as they are in the form of fine particles, they pass through the diesel filters and are deposited inside the injectors.
  • the development of an engine test is described and allows the deposits to be reproduced.
  • the present invention makes it possible to overcome the drawbacks indicated above.
  • the applicant showed that the combination of two particular additives allowed a surprising synergistic effect to be obtained in particular for controlling deposits on the injectors.
  • the present invention proposes compositions of additives capable of tangibly improving the control of deposits, in particular of the lacquering type of diesel and/or bio diesel fuels.
  • the present invention also relates to compositions of additives that also improve the control of deposits of the coking type and/or the lubricating properties of diesel and/or bio diesel fuel.
  • the present invention relates to a composition of fuel additives comprising at least:
  • the mass ratio of the first to the second additive is comprised between 1:100 and 100:1, preferably between 1:10 and 10:1, even more preferably between 1:2 and 2:1.
  • the triazole derivative has the formula (I) in which R 3 and R 4 are identical or different and represent, independently of one another, a group selected from the group consisting of a hydrogen atom and an aliphatic hydrocarbon group having a number-average molecular weight (Mn) comprised between 200 and 3000.
  • the triazole derivative is represented by the following formula (II) and/or (III):
  • R 1 , R 3 and R 4 are as defined above.
  • the triazole derivative is obtained by reaction of an aminotriazole of the following formula (IV) with a diacid of the following formula (V) and/or a succinic anhydride of the following formula (VI):
  • the quaternizing agent is selected from the group constituted by the dialkyl sulphates, the carboxylic acid esters, the alkyl halides, the benzyl halides, the hydrocarbon carbonates and the hydrocarbon epoxides optionally mixed with an acid, alone or in a mixture.
  • the nitrogen containing compound comprises a product of reaction of an acylating agent substituted with a hydrocarbon group and an amine of the following formula (VII) or (VIII):
  • the composition of additives further comprises a third additive comprising at least 50% by mass of a compound A selected from the partial esters of polyols and of saturated or unsaturated, linear or branched, cyclic or acyclic C 4 to C 36 monocarboxylic aliphatic hydrocarbons, said partial esters being able to be used alone or in a mixture.
  • said compound A comprises x ester unit(s), y hydroxyl unit(s) and z ether unit(s), x, y and z being integers such that x varies from 1 to 10, y varies from 1 to 10, and z varies from 0 to 6.
  • the distribution of ester, hydroxyl and ether units in said compound A is such that x varies from 1 to 4, y varies from 1 to 7 and z varies from 1 to 3.
  • compound A is obtained by esterification between:
  • the fatty acids are selected from the group constituted by stearic, isostearic, linolenic, oleic, linoleic, behenic, arachidonic, ricinoleic, palmitic, myristic, lauric, and capric acids, used alone or in a mixture.
  • the polyol is selected from the polyols comprising more than three hydroxyl functions and the polyols comprising at least one heterocycle with 5 or 6 atoms, preferably heterocycles with 4 to 5 carbon atoms and one oxygen atom, optionally substituted with hydroxyl groups.
  • the polyol is selected from the group consisting of erythritol, xylitol, arabitol, ribitol, sorbitol, maltitol, isomaltitol, lactitol, volemitol, mannitol, pentaerythritol, 2-hydroxymethyl-1,3-propanediol, 1,1,1-tri(hydroxymethyl)ethane, trimethylolpropane, sorbitan and the carbohydrates such as sucrose, fructose, maltose, glucose and saccharose.
  • compound A is selected from the sorbitan partial esters, preferably the sorbitan mono-, di- and triesters, used alone or in a mixture, more preferably the sorbitan partial esters comprising more than 40% by mass of sorbitan triesters.
  • compound A is selected from the monoester(s) and/or diester(s) of polyglycerols having from 2 to 5 glycerol units per molecule.
  • compound A is selected from the monoester(s) and/or diester(s) of polyglycerols derived from fatty acid(s), having more than 50% by number of fatty chains comprising between 12 and 24 carbon atoms, preferably compound A is selected from the monoester(s) and/or diester(s) of diglycerol and/or of triglycerol, more preferably from the partial esters of diglycerol and/or of triglycerol comprising at least 50% by mass of monoester(s) and/or of diester(s) of oleic acid and of diglycerol.
  • the present invention also relates to the use of a composition of additives according to the present invention, in a diesel fuel having a sulphur content less than or equal to 500 ppm by mass, preferably comprising a bio diesel.
  • the present invention also relates to a diesel fuel having a sulphur content less than or equal to 500 ppm by mass comprising at least 5 ppm by mass of a composition of additives according to the present invention, preferably a fuel comprising up to 30% by volume of bio diesel.
  • the fuel additionally comprises at least one or more other additives selected from the antioxidants, combustion improvers, corrosion inhibitors, low temperature performance additives, dyes, demulsifiers, metal deactivators, antifoaming agents, cetane number improvers, lubricity additives, co-solvents and compatibilizing agents.
  • the concentration by mass of each first and second additive and optionally third additive varies from 5 to 5000 ppm.
  • the present invention also relates to the use of a diesel fuel according to the present invention in a diesel engine, for improving the performance of said engine, in particular for:
  • the engine is a direct-injection engine, preferably with a high-pressure injection system (“common-rail”).
  • FIG. 1 is a photograph of a high-pressure, direct-injection diesel engine injector
  • FIG. 2 is a photograph of a needle of a direct-injection diesel engine injector, fouled with deposits of the soap and/or lacquer type (“lacquering”);
  • FIG. 3 is a photograph of a nozzle of an indirect-injection diesel engine injector, fouled with deposits of the coke type (“coking”);
  • FIG. 4 is a photograph of a needle of a direct-injection diesel engine injector, fouled with deposits of the soap and/or lacquer type (“lacquering”).
  • the present invention relates to a composition of additives comprising at least a first and a second additive, and optionally a third additive.
  • the present invention also relates to the use of such a composition of additives in a diesel fuel having a sulphur content less than or equal to 500 ppm by mass, preferably comprising a bio diesel.
  • the first additive comprises a triazole derivative of the following formula (I):
  • R 1 is selected from the group consisting of a hydrogen atom, a linear or branched C 1 to C 8 , preferably C 1 to C 4 , more preferably C 1 to C 2 , aliphatic hydrocarbon group and a carboxyl group (—CO 2 H).
  • R 1 is a hydrogen atom.
  • R 2 and R 5 are identical or different and represent, independently of one another, a group selected from the group consisting of a hydrogen atom and a linear or branched, saturated or unsaturated C 1 to C 33 , preferably C 1 to C 21 aliphatic hydrocarbon group, optionally comprising one or more oxygen atoms in the form of a carbonyl function (—CO—) and/or carboxyl function (—CO 2 H), said R 2 and R 5 groups optionally forming together a ring with 5 to 8 atoms comprising nitrogen, to which R 2 is bound, it being understood that in this case R 2 and R 5 then constitute one and the same linear or branched, saturated or unsaturated, C 1 to C 33 , preferably C 1 to C 21 aliphatic hydrocarbon group, optionally substituted with one or more oxygen atoms in the form of a carbonyl function (—CO—) and/or carboxyl function (—CO 2 H).
  • R 3 and R 4 are identical or different and represent, independently of one another, a group selected from the group consisting of a hydrogen atom and a linear or branched, saturated or unsaturated, cyclic or acyclic, aliphatic hydrocarbon group, having from 2 to 200 carbon atoms, preferably from 14 to 200 carbon atoms, more preferably from 50 to 170 carbon atoms, even more preferably between 60 and 120 carbon atoms.
  • the triazole derivative has the formula (I) in which R 3 and R 4 are identical or different and represent, independently of one another, a group selected from the group consisting of a hydrogen atom and an aliphatic hydrocarbon group having a number-average molecular weight (M n ) comprised between 200 and 3000, preferably between 400 and 3000, more preferably between 400 and 2500, even more preferably between 400 and 1500 or between 500 and 1500.
  • M n number-average molecular weight
  • Said aliphatic hydrocarbon group is preferably a polyisobutylene group (also called polyisobutene, denoted PIB) having a number-average molecular weight (M n ) comprised between 200 and 3000, preferably between 400 and 3000, more preferably between 400 and 2500, even more preferably between 400 and 1500 or between 500 and 1500.
  • R 3 and R 4 preferably represent, respectively, a hydrogen atom and a PIB group as described above or vice versa.
  • the triazole derivative is represented by the following formula (II):
  • R 1 , R 3 and R 4 are as defined above.
  • the triazole derivative is represented by the following formula (III):
  • R 1 , R 3 and R 4 are as defined above.
  • the first additive is a mixture of triazole derivatives of formulae (II) and (III) as defined above.
  • the triazole derivative may be in the form of a mixture of derivatives in the closed form (II) and open form (III).
  • the mass ratio (II):(III) in said mixture of the triazole derivatives in the closed and open form respectively may be comprised between 1:100 and 100:1, preferably between 50:10 and 90:10, more preferably between 91:9 and 99:1.
  • a first additive comprising less than 10% by mass of triazole derivatives of formula (III) in the open form will be preferred.
  • the triazole derivative may be obtained by any known process, in particular by reaction of an aminotriazole of the following formula (IV) with a diacid of the following formula (V) and/or a succinic anhydride of the following formula (VI):
  • R 1 , R 3 and R 4 are as defined above.
  • the second additive comprises a quaternary ammonium salt obtained by reaction of a nitrogen containing compound comprising a tertiary amine function with a quaternizing agent.
  • quaternary ammonium salts and the process for the preparation thereof are described in U.S. Pat. Nos. 4,253,980, 3,778,371, 4,171,959, 4,326,973, 4,338,206, 5,254,138 and PCT Patent Publication No. WO2010/132259, cited by way of examples and/or incorporated by reference in the present application.
  • the nitrogen containing compound (a) is selected from the product of reaction of an acylating agent substituted with a hydrocarbon group, with a compound comprising at least one tertiary amine group and a group selected from the primary and secondary amines or the alcohols.
  • the nitrogen-containing compound (a) is preferably the product of reaction of an acylating agent substituted with a hydrocarbon group, with a compound comprising both an oxygen atom or a nitrogen atom capable of condensing with said acylating agent, and a tertiary amine group.
  • the acylating agent is, advantageously, selected from the mono- or polycarboxylic acids substituted with a hydrocarbon group and their derivatives, alone or in a mixture.
  • the acylating agent is, for example, selected from the succinic, phthalic and propionic acids substituted with a hydrocarbon group.
  • the hydrocarbon substituent of the acylating agent preferably comprises at least 8, preferably at least 12 carbon atoms, for example between 30 or 50 carbon atoms. Said hydrocarbon substituent may comprise up to approximately 200 carbon atoms.
  • the hydrocarbon substituent of the acylating agent preferably has a number-average molecular weight (M n ) comprised between 170 and 2800, for example between 250 and 1500, more preferably between 500 and 1500, and even more preferably between 500 and 1100.
  • M n number-average molecular weight
  • a range of values of M n comprised between 700 and 1300 is particularly preferred, for example from 700 to 1000.
  • hydrocarbon groups substituting the acylating agent we may mention the n-octyl, n-decyl, n-dodecyl, tetrapropenyl, n-octadecyl, oleyl, octadecyl or triacontyl groups.
  • the hydrocarbon substituent of the acylating agent may be obtained from homo- or inter-polymers (for example copolymers, terpolymers) of mono- and diolefins having from 2 to 10 carbon atoms, for example from ethylene, propylene, 1-butene, isobutene, butadiene, isoprene, 1-hexene or 1-octene.
  • these olefins are 1-mono-olefins.
  • the hydrocarbon substituent of the acylating agent may also be derivatives of halogenated analogues (for example chlorinated or brominated) of these homo- or inter-polymers.
  • the hydrocarbon substituent of the acylating agent may be obtained from other sources, for example starting from monomers of alkenes of high molecular weight (for example, 1-tetracontene) and their chlorinated or hydrochlorinated analogues, from aliphatic petroleum fractions, for example the paraffin waxes, their cracked, chlorinated and/or hydrochlorinated analogues, from white oils, from synthetic alkenes, for example produced by a Ziegler-Natta process (for example the polyethylene greases) and from other sources known to a person skilled in the art. Any unsaturation in the hydrocarbon group of the acylating agent may also be reduced or removed by hydrogenation by any known process.
  • monomers of alkenes of high molecular weight for example, 1-tetracontene
  • aliphatic petroleum fractions for example the paraffin waxes, their cracked, chlorinated and/or hydrochlorinated analogues
  • white oils from synthetic alkenes, for example produced by
  • hydrocarbon group is meant any group having a carbon atom attached directly to the rest of the molecule and mainly having an aliphatic hydrocarbon character.
  • Hydrocarbon groups according to the invention may also contain non-hydrocarbon groups. For example, they may contain up to one non-hydrocarbon group per ten carbon atoms provided that the non-hydrocarbon group does not significantly alter the mainly hydrocarbon character of the group.
  • the hydroxyl groups, the halogens (in particular the chloro and fluoro groups), the alkoxy, alkylmercapto, and alkylsulphoxy groups are well known to a person skilled in the art.
  • hydrocarbon substituents not containing such non-hydrocarbon groups, and having a purely aliphatic hydrocarbon character will be preferred.
  • the hydrocarbon substituent of the acylating agent is preferably essentially saturated, i.e. it does not contain more than one unsaturated carbon-carbon bond for each section of ten carbon-carbon single bonds present.
  • the hydrocarbon substituent of the acylating agent advantageously contains not more than one non-aromatic unsaturated carbon-carbon bond to every 50 carbon-carbon bonds present.
  • the hydrocarbon substituent of the acylating agent is preferably selected from the polyisobutenes known in the prior art.
  • the acylating agent substituted with a hydrocarbyl group is a polyisobutenyl succinic anhydride (PIBSA).
  • PIBSA polyisobutenyl succinic anhydride
  • the preparation of polyisobutenyl succinic anhydrides (PIBSA) is widely described in the literature. The methods comprising the reaction between polyisobutenes (FIB) and maleic anhydride described in U.S. Pat. Nos.
  • the polyisobutenyl succinic anhydride may be prepared by mixing a polyolefin with maleic anhydride and then passing chlorine through the mixture (GB949 981).
  • the polyisobutenes (PIBs) referred to as highly reactive will be used.
  • highly reactive polyisobutenes (PIBs) is meant polyisobutenes (FIB) in which at least 50%, preferably at least 70% or more, of the terminal olefinic double bonds are of the vinylidene type as described in document EP0565285.
  • the preferred PIBs are those having more than 80 mol % and up to 100 mol % of terminal vinylidene groups as described in document EP1344785.
  • Internal olefin means any olefin mainly containing a non-alpha double bond, which is a beta olefin or with a higher position.
  • these materials are essentially beta-olefins or olefins of higher position, for example containing less than 10% by mass of alpha-olefin, advantageously less than 5% by mass or less than 2% by mass.
  • the internal olefins may be prepared by isomerization of alpha-olefins by any known process.
  • the compound comprising both an oxygen atom or a nitrogen atom capable of condensing with the acylating agent and a tertiary amine group may, for example, be selected from the group consisting of: N,N-dimethylaminopropylamine, N,N-diethylaminopropylamine, N,N-dimethylaminoethylamine.
  • Said compound may moreover be selected from the heterocyclic compounds substituted with alkylamines such as 1-(3-aminopropyl)imidazole and 4-(3-aminopropyl)morpholine, 1-(2-aminoethyl)piperidine, 3,3-diamino-N-methyldipropylamine, and 3′3-bisamino(N,N-dimethylpropylamine).
  • alkylamines such as 1-(3-aminopropyl)imidazole and 4-(3-aminopropyl)morpholine, 1-(2-aminoethyl)piperidine, 3,3-diamino-N-methyldipropylamine, and 3′3-bisamino(N,N-dimethylpropylamine).
  • the compound comprising both an oxygen atom or a nitrogen atom capable of condensing with the acylating agent and a tertiary amine group may also be selected from the alkanolamines, including, but not limited to, triethanolamine, trimethanolamine, N,N-dimethylaminopropanol, N,N-dimethylaminoethanol, N,N-diethylaminopropanol, N,N-diethylaminoethanol, N,N-diethylaminobutanol, N,N,N-tris(hydroxyethyl)amine, N,N,N-tris(hydroxymethyl)amine, N,N,N-tris(aminoethyl)amine, N,N-dibutylaminopropylamine and N,N,N′-trimethyl-N′-hydroxyethyl-bisaminoethyl ether, N,N-bis(3-dimethylamino-propyl)-N-
  • the nitrogen containing compound (a) comprises a product of reaction of an acylating agent substituted with a hydrocarbon group and an amine of the following formula (VII) or (VIII):
  • R 8 is advantageously a hydrogen atom or a C 1 to C 16 alkyl group, preferably a C 1 to C 10 alkyl group, even more preferably a C 1 to C 6 alkyl group.
  • R 8 may, for example, be selected from the group consisting of hydrogen, methyl, ethyl, propyl, butyl and isomers thereof.
  • R 8 is a hydrogen atom.
  • m is preferably equal to 2 or 3, more preferably equal to 2; n is preferably an integer between 0 and 15, more preferably between 0 and 10, even more preferably between 0 and 5.
  • n is 0 and the compound of formula (VIII) is an alcohol.
  • the nitrogen containing compound (a) is the product of reaction of the acylating agent substituted with a hydrocarbon group with the diamine of formula (VII).
  • R 6 and R 7 may represent, independently of one another, a C 1 to C 16 alkyl group, preferably a C 1 to C 10 alkyl group to form an alkyl group.
  • R 6 and R 7 may represent, independently of one another, a methyl, ethyl, propyl, butyl, pentyl, hexyl, heptyl, octyl group or isomers thereof.
  • R 6 and R 7 represent, independently of one another, a C 1 to C 4 group, preferably a methyl group.
  • X preferably represents an alkylene group having 1 to 16 carbon atoms, preferably from 1 to 12 carbon atoms, more preferably from 1 to 8 carbon atoms, for example from 2 to 6 carbon atoms or from 2 to 5 carbon atoms.
  • X advantageously represents an ethylene, propylene or butylene group, in particular a propylene group.
  • the quaternary ammonium salt of the second additive may for example be obtained by the preparation process described in international application WO2006/135881.
  • the nitrogen containing compound (a) is the product of reaction of a derivative of succinic acid substituted with a hydrocarbon group, preferably a polyisobutenyl succinic anhydride, and an alcohol or an amine also comprising a tertiary amine group.
  • a hydrocarbon group preferably a polyisobutenyl succinic anhydride
  • an alcohol or an amine also comprising a tertiary amine group.
  • the succinic acid derivative substituted with a hydrocarbon group reacts with the amine also comprising a tertiary amine group to form a succinimide (closed form).
  • reaction of the succinic acid derivative and the amine may lead under certain conditions to a succinamide, i.e. a compound comprising an amide group and a carboxylic acid group (open form).
  • an alcohol also comprising a tertiary amine group reacts with the succinic acid derivative to form an ester.
  • This ester molecule also comprises a free carboxyl group —CO 2 H (open form).
  • the nitrogen-containing compound (a) may be the product of reaction of a succinic acid derivative and an amine or an alcohol which is an ester or an amide and which further also comprises an unreacted carboxyl group —CO 2 H (open form).
  • the nitrogen containing compound (b) is selected from a product of the Mannich reaction comprising a tertiary amine group.
  • the preparation of quaternary ammonium salts formed from a nitrogen containing compound, in particular from nitrogen containing compound (b), is described for example in U.S. Patent Publication No. 2008/0052985.
  • the product of the Mannich reaction comprising a tertiary amine group is prepared by reaction of a phenol substituted with a hydrocarbon group, an aldehyde and an amine.
  • the hydrocarbon substituent of said phenol may contain from 6 to 400 carbon atoms, advantageously from 30 to 180 carbon atoms, for example from 10 to 110, or from 40 to 110 carbon atoms.
  • the hydrocarbon substituent of said phenol may be derived from an olefin or a polyolefin.
  • the alpha-olefins such as n ⁇ 1-decene may be mentioned.
  • the polyolefins forming the hydrocarbon substituent of the phenol may be prepared by polymerization of monomers of olefins by any known process of polymerization.
  • the polyolefins are selected from the polyisobutylenes having a number-average molecular weight (Mn) between 400 and 3000, preferably between 400 and 2500, more preferably between 400 and 1500 or between 500 and 1500.
  • Mn number-average molecular weight
  • the phenol substituted with a hydrocarbon group may be prepared by alkylation of phenol with an olefin or polyolefin described above, such as a polyisobutylene or polypropylene, using conventional methods of alkylation.
  • the phenol may be substituted with one or more alkyl groups of low molecular weight, for example a phenol bearing one or more alkyl chains with fewer than 28 carbon atoms, preferably with fewer than 24 carbon atoms, more preferably with fewer than 20 carbon atoms, even more preferably with fewer than 18 carbon atoms, even more preferably with 16 carbon atoms and even more preferably with 14 carbon atoms.
  • a monoalkyl phenol preferably having from 4 to 20 carbon atoms, preferably from 6 to 18, more preferably from 8 to 16, even more preferably from 10 to 14 carbon atoms, for example a phenol substituted with a C 12 alkyl group, will be preferred.
  • the aldehyde used for forming the product of the Mannich reaction may comprise from 1 to 10 carbon atoms, and is generally formaldehyde or its reactive equivalents such as Formalin (methanol and formaldehyde) or para-formaldehyde.
  • the amine used for forming the product of the Mannich reaction may be a monoamine or a polyamine.
  • ethylamine, dimethylamine, diethylamine, n-butylamine, dibutylamine, allylamine, isobutylamine, cocoamine, stearylamine, laurylamine, methyllaurylamine, oleylamine, N-methyloctylamine, dodecylamine, diethanolamine, morpholine and octadecylamine may be mentioned as monoamines.
  • the polyamines are selected from the compounds comprising two or more amine groups.
  • the polyalkylene polyamines in which the alkylene group has for example from 1 to 6, preferably from 1 to 4, more preferably from 2 to 3 carbon atoms may be mentioned as polyamines.
  • the preferred polyamines are the polyethylene-polyamines.
  • the polyamine may comprise from 2 to 15 nitrogen atoms, preferably from 2 to 10 nitrogen atoms, preferably 2 to 8 nitrogen atoms.
  • the amine used for forming the product of the Mannich reaction comprises a diamine, which preferably comprises a primary or secondary amine function taking part in the Mannich reaction and a tertiary amine.
  • the nitrogen-containing compound (b) comprises the product obtained directly by the Mannich reaction, and comprising a tertiary amine.
  • the amine comprises a single primary or secondary amine function that is involved in the Mannich reaction and a quaternizable tertiary amine.
  • the amine comprises a primary or secondary amine capable of taking part in the Mannich reaction, and a quaternizable tertiary amine.
  • the nitrogen containing compound (b) may be obtained by a Mannich reaction and then subjected to a reaction for obtaining a tertiary amine, for example a process using an intermediate comprising a secondary amine and obtained by the Mannich reaction, which is then modified, for example by alkylation, to give a secondary amine.
  • the nitrogen containing compound (c) is selected from the amines substituted with a polyalkene group (also called polyalkylene) having at least one tertiary amine group.
  • a polyalkene group also called polyalkylene
  • Preparation of quaternary ammonium salts formed from a nitrogen containing compound (c) is described for example in U.S. Patent Publication No 2008/0113890.
  • the amines substituted with a polyalkene group having at least one tertiary amine group may be derived from polyolefin and amine, for example ammonia, the monoamines, the polyamines, alone or in combination. Said amines may be prepared by any known process, for example those described in U.S. Patent Publication No. 2008/0113890.
  • reaction of a halogenated olefinic polymer with an amine reaction of a hydroformylated olefin with a polyamine followed by hydrogenation of the reaction product; conversion of a polyalkene to the corresponding epoxide followed by conversion of the epoxide to aminated polyalkene by reductive amination; hydrogenation of a ⁇ -aminonitrile; and hydroformylation of a polybutene or polyisobutylene in the presence of a catalyst, CO and H 2 at high pressure and temperature may be mentioned.
  • the olefinic monomers from which the olefinic polymers are derived comprise the polymerizable olefinic monomers characterized by the presence of one or more ethylenic unsaturations, for example ethylene, propylene, 1-butene, isobutene, 1-octene, 1,3-butadiene and isoprene.
  • the olefinic monomers are generally polymerizable terminal olefins. However, polymerizable internal olefinic monomers may also be used for forming the polyalkenes.
  • the terminal and internal olefinic monomers that may be used for preparing the polyalkenes by any known process are: ethylene; propylene; the butenes, including 1-butene, 2-butene and isobutylene; 1-pentene; 1-hexene; 1-heptene; 1-octene; 1-nonene; 1-decene; 2-pentene; propylene tetramer; diisobutylene; isobutylene trimer; 1,2-butadiene; 1,3-butadiene; 1,2-pentadiene; 1,3-pentadiene; 1,4-pentadiene; isoprene; 5-hexadiene; 2-methyl-5-propyl-1-hexene; 3-pentene; 4-octene and 3,3-dimethyl-1-pentene.
  • Amines substituted with derivatives of polyisobutylene will preferably be selected.
  • the amines used for preparing the amines substituted with a polyalkene group may be selected from ammonia, the monoamines, the polyamines alone or in mixtures, including mixtures of different monoamines, mixtures of different polyamines, and mixtures of monoamines and polyamines (including the diamines).
  • Said amines comprise aliphatic, aromatic, and heterocyclic hydrocarbons and the carbocyclic amines.
  • the monomers and the polyamines advantageously comprise at least one primary or secondary amine.
  • the monoamines are generally substituted with a hydrocarbon group having from 1 to approximately 50 carbon atoms, preferably from 1 to 30 carbon atoms.
  • the saturated aliphatic hydrocarbon substituents are particularly preferred.
  • methylamine, ethylamine, diethylamine, 2-ethylhexylamine, di(2-ethylhexyl)amine, n-butylamine, di-n-butylamine, allylamine, isobutylamine, cocoamine, stearylamine, laurylamine, methyllaurylamine and oleylamine may be mentioned.
  • the aromatic monoamines comprise the monoamines in which a carbon atom having an aromatic cyclic structure is attached directly to the amine nitrogen. Examples of aromatic monoamines comprise aniline, di(para-methylphenyl)amine, naphthylamine and N-(n-butyl)aniline.
  • Examples of aromatic monoamines substituted with aliphatic, cycloaliphatic and heterocyclic hydrocarbon groups comprise para-dodecylaniline, cyclohexyl-naphthylamine and thienylaniline, respectively.
  • the monoamines according to the present invention also comprise the hydroxyamines.
  • ethanolamine, di-3-propanolamine, 4-hydroxybutylamine, diethanolamine and N-methyl-2-hydroxypropylamine may be mentioned.
  • the polyamines may also be selected from the amines substituted with polyalkene groups.
  • the polyamine may be aliphatic, cycloaliphatic, heterocyclic or aromatic.
  • the alkylene polyamines, the polyamines with hydroxy substitution, the arylpolyamines and the heterocyclic polyamines may be mentioned.
  • the ethylenic polyamines are preferred for reasons of cost and efficiency.
  • the polyamines with hydroxy substitution comprise the hydroxyalkylated alkene polyamines having one or more hydroxyalkyl substituents on the nitrogen atoms and that may be prepared by reaction of the alkene polyamines with one or more alkene oxides.
  • N-(2-hydroxyethyl)ethylenediamine, N,N-bis(2-hydroxyethyl)ethylenediamine, 1-(2-hydroxyethyl)piperazine, monohydroxypropyl-diethylenetriamine, dihydroxypropyl-tetraethylenepentamine and N-(3-hydroxybutyl)-tetramethylenediamine may be mentioned.
  • arylpolyamines are analogues of the aromatic monoamines described above except for the presence in their structure of another amino nitrogen.
  • N,N′-di-n-butyl-para-phenylenediamine and bis(para-aminophenyl)methane may be mentioned.
  • the mono- and heterocyclic polyamines will be known to a person skilled in the art.
  • N-aminopropylmorpholine, N-aminoethylpiperazine, and N,N′-diaminoethylpiperazine may be mentioned.
  • the hydroxy-heterocyclic polyamines may also be used, for example N-(2-hydroxyethyl)cyclohexylamine, 3-hydroxycyclopentylamine, parahydroxy-aniline and N-hydroxyethylpiperazine.
  • Examples of amines substituted with polyalkene groups may comprise: polypropylene amine, polybutene amine, N,N-dimethyl-polyisobutylene-amine, N-polybutene-morpholine, N-polybutene-ethylenediamine, N-polypropylene trimethylenediamine, N-polybutene-diethylenetriamine, N′,N′-polybutene-tetraethylenepentamine and N,N-dimethyl-N′-polypropylene-1,3-propylenediamine.
  • the number-average molecular weight (M n ) of the amines with polyalkene substitution may range from 500 to 5000, preferably from 500 to 3000, for example from 1000 to 1500.
  • All the amines with polyalkene substitution described above that are primary or secondary amines may be alkylated to form tertiary amine functions using alkylating agents by any known process.
  • the quaternary ammonium salt of the second additive according to the present invention is obtained directly by reaction between the nitrogen-containing compound described above comprising a tertiary amine function and a quaternizing agent.
  • the quaternizing agent is selected from the group constituted by the dialkyl sulphates, the carboxylic acid esters; the alkyl halides, the benzyl halides, the hydrocarbon carbonates, and the hydrocarbon epoxides optionally mixed with an acid, alone or in a mixture.
  • quaternizing agent containing such an element
  • a quaternary ammonium salt formed by reaction with an alkyl halide may then be reacted with sodium hydroxide and the sodium halide salt may be removed by filtration.
  • the quaternizing agent may comprise halides such as chloride, iodide or bromide; hydroxides; sulphonates; bisulphites; alkyl sulphates such as dimethyl sulphate; sulphones; phosphates; C 1 -C 12 alkyl phosphates; C 1 -C 12 dialkyl phosphates; borates; C 1 -C 12 alkyl borates; nitrites; nitrates; carbonates; bicarbonates; alkanoates; C 1 -C 12 O,O-dialkyldithiophosphates, alone or in a mixture.
  • halides such as chloride, iodide or bromide
  • hydroxides such as chloride, iodide or bromide
  • sulphonates such as dimethyl sulphate
  • sulphones such as dimethyl sulphate
  • phosphates C 1 -C 12 alkyl phosphates
  • the quaternizing agent may be derived from dialkyl sulphates such as dimethyl sulphate, from N-oxides, from sulphones such as propane- and butane-sulphone, from alkyl halides, from acyl or from aralkyl such as methyl and ethyl chloride, benzyl bromide, iodide or chloride, and the hydrocarbon carbonates (or alkyl carbonates). If the acyl halide is benzyl chloride, the aromatic ring is optionally substituted with one or more alkyl or alkenyl groups.
  • the hydrocarbon groups (alkyls) of the hydrocarbon carbonates may contain from 1 to 50, from 1 to 20, from 1 to 10 or 1 to 5 carbon atoms per group.
  • the hydrocarbon carbonates contain two hydrocarbon groups, which may be identical or different.
  • hydrocarbon carbonates dimethyl or diethyl carbonate may be mentioned.
  • the quaternizing agent is selected from the hydrocarbon epoxides represented by the following formula (IX):
  • R 9 , R 10 , R 11 and R 12 may be identical or different and represent, independently, a hydrogen atom or a C 1 -C 50 hydrocarbon group.
  • R 9 , R 10 , R 11 and R 12 may be identical or different and represent, independently, a hydrogen atom or a C 1 -C 50 hydrocarbon group.
  • styrene oxide, ethylene oxide, propylene oxide, butylene oxide, stilbene oxide and the C 1 -C 50 epoxides may be mentioned.
  • Styrene oxide is particularly preferred.
  • hydrocarbon epoxides of this kind are used as quaternizing agent in combination with an acid, for example with acetic acid.
  • an acid for example with acetic acid.
  • the hydrocarbon epoxide may be used alone as quaternizing agent without additional acid. Without being bound by this hypothesis, it would seem that the presence of the carboxylic acid function in the molecule promotes formation of the quaternary ammonium salt.
  • a protic solvent is used for preparing the quaternary ammonium salt.
  • the protic solvents such as water, the alcohols (including the polyhydric alcohols) may be used alone or in a mixture.
  • the preferred protic solvents have a dielectric constant greater than 9.
  • the appropriate quaternary ammonium salts prepared from amides or esters and derivatives of succinic acid are described in WO2010/132259.
  • the quaternizing agent comprises a compound of formula (X):
  • R 13 is an alkyl, alkenyl, aryl and aralkyl group, optionally substituted
  • R 14 is a C 1 to C 22 alkyl, aryl or alkylaryl group.
  • the compound of formula (X) is a carboxylic acid ester capable of reacting with a tertiary amine to form a quaternary ammonium salt.
  • Compounds of formula (X) are selected, for example, from the esters of carboxylic acids having a pKa of 3.5 or less.
  • the compound of formula (X) is preferably selected from the esters of substituted aromatic carboxylic acid, of ⁇ -hydroxycarboxylic acid and of polycarboxylic acid.
  • the ester is an ester of substituted aromatic carboxylic acid of formula (X) in which R 13 is a substituted aryl group.
  • R 13 is a substituted aryl group having 6 to 10 carbon atoms, preferably a phenyl or naphthyl group, more preferably a phenyl group.
  • R 13 is advantageously substituted with one or more groups selected from the carboalkoxy, nitro, cyano, hydroxy, SR 15 and NR 15 R 16 radicals.
  • Each of the R 15 and R 16 groups may be a hydrogen atom or an alkyl, alkenyl, aryl or carboalkoxy group, optionally substituted.
  • Each of the R 15 and R 16 groups represents, advantageously, a hydrogen atom or a C 1 to C 22 alkyl group, optionally substituted, preferably a hydrogen atom or a C 1 to C 16 alkyl group, more preferably a hydrogen atom or a C 1 to C 10 alkyl group, even more preferably a hydrogen atom or a C 1 to C 4 alkyl group.
  • R 15 is preferably a hydrogen atom and R 16 a hydrogen atom or a C 1 to C 4 group.
  • R 15 and R 16 are both a hydrogen atom.
  • R 13 is an aryl group substituted with one or more groups selected from the hydroxyl, carboalkoxy, nitro, cyano and NH 2 radicals.
  • R 13 may be a polysubstituted aryl group, for example trihydroxyphenyl.
  • R 13 is a monosubstituted aryl group, preferably ortho-substituted.
  • R 13 is, for example, substituted with a group selected from the OH, NH 2 , NO 2 or COOMe radicals, preferably OH or NH 2 .
  • R 13 is preferably a hydroxy-aryl group, in particular 2-hydroxyphenyl.
  • R 14 is an alkyl or alkylaryl group.
  • R 14 may be a C 1 to C 16 , preferably C 1 to C 10 , advantageously C 1 to C 8 alkyl group.
  • R 14 may be a C 1 to C 16 , preferably C 1 to C 10 , advantageously C 1 to C 8 alkylaryl group.
  • R 14 may for example be selected from the methyl, ethyl, propyl, butyl, pentyl, benzyl groups or isomers thereof.
  • R 14 is a benzyl or methyl group, more preferably methyl.
  • a particularly preferred compound of formula (X) is methyl salicylate.
  • the compound of formula (X) is an ester of an ⁇ -hydroxycarboxylic acid of the following formula:
  • R 17 and R 18 are identical or different, and are selected independently from the group consisting of the hydrogen atom, the alkyl, alkenyl, aryl or aralkyl groups.
  • R 17 and R 18 are identical or different, and are selected independently from the group consisting of the hydrogen atom, the alkyl, alkenyl, aryl or aralkyl groups.
  • Such compounds are described for example in document EP 1254889.
  • Examples of compounds of formula (X) in which R 13 COO is the residue of an ⁇ -hydroxycarboxylic acid comprise the methyl, ethyl, propyl, butyl, pentyl, hexyl, phenyl, benzyl or allyl esters of 2-hydroxy-isobutyric acid; the methyl, ethyl, propyl, butyl, pentyl, hexyl, benzyl, phenyl or allyl esters of 2-hydroxy-2-methylbutyric acid; the methyl, ethyl, propyl, butyl, pentyl, hexyl, benzyl, phenyl or allyl esters of 2-hydroxy-2-ethylbutyric acid; the methyl, ethyl, propyl, butyl, pentyl, hexyl, benzyl, phenyl or allyl esters of 2-hydroxy-2-ethylbutyric acid
  • the preferred compound is methyl-2-hydroxyisobutyrate.
  • the compound of formula (X) is an ester of a polycarboxylic acid comprising the dicarboxylic acids and the carboxylic acids having more than two acid functions.
  • the carboxyl functions are preferably all in the esterified form.
  • the preferred esters are the C 1 to C 4 alkyl esters.
  • the compound of formula (X) may be selected from the oxalic acid diesters, the phthalic acid diesters, the maleic acid diesters, the malonic acid diesters or the citric acid diesters.
  • the compound of formula (X) is dimethyl oxalate.
  • the compound of formula (X) is a carboxylic acid ester having a pKa below 3.5. For the cases where the compound comprises more than one acid group, reference will be made to the first dissociation constant.
  • the compound of formula (X) may be selected from one or more carboxylic acid esters selected from oxalic acid, phthalic acid, salicylic acid, maleic acid, malonic acid, citric acid, nitrobenzoic acid, aminobenzoic acid and 2,4,6-trihydroxybenzoic acid.
  • carboxylic acid esters selected from oxalic acid, phthalic acid, salicylic acid, maleic acid, malonic acid, citric acid, nitrobenzoic acid, aminobenzoic acid and 2,4,6-trihydroxybenzoic acid.
  • the preferred compounds of formula (X) are dimethyl oxalate, 2-methyl nitrobenzoate and methyl salicylate.
  • the quaternary ammonium salt according to the invention is formed by reaction of 2-methylhydroxybenzoate or styrene oxide with the reaction product of a polyisobutenyl succinic anhydride the polyisobutylene group (PIB) of which has a number-average molecular weight (Mn) between 700 and 1000 and dimethyl-aminopropylamine.
  • the composition of additives comprises the first additive as described above preferably comprising a triazole derivative of formula (II) and/or (III) and the second additive comprising a quaternary ammonium salt obtained from the nitrogen-containing compound (a) described above.
  • the composition of additives described above may further comprise a third additive.
  • the third additive comprises at least 50% by mass of a compound A selected from the partial esters of polyols and of saturated or unsaturated, linear or branched, cyclic or acyclic, C 4 to C 36 , preferably C 12 -C 24 , more preferably C 16 -C 20 , monocarboxylic aliphatic hydrocarbons, said partial esters being able to be used alone or in a mixture.
  • Compound A preferably comprises x ester units, y hydroxyl units and z ether units, x, y and z being integers such that x varies from 1 to 10, y varies from 1 to 10, and z varies from 0 to 6. According to a particular embodiment, x varies from 1 to 10, y varies from 3 to 10, and z varies from 0 to 6. According to another particular embodiment x varies from 1 to 4, y varies from 1 to 7 and z varies from 1 to 3. Advantageously, x varies from 2 to 4.
  • partial esters of polyols are known per se; they may for example be prepared by esterification of fatty acid(s) and of linear and/or branched polyols optionally comprising (hetero)cycles with 5 to 6 atoms bearing hydroxyl functions. Generally this type of synthesis leads to a mixture of mono-, di-, tri- and optionally of tetra-esters as well as small quantities of fatty acid(s) and unreacted polyols.
  • compound A is obtained by esterification of one or more C 4 to C 36 fatty acid(s), preferably C 10 -C 24 , more preferably C 12 -C 24 , optionally comprising one or more ethylenic bonds, and of a linear or branched, cyclic or acyclic polyol, optionally comprising a heterocycle with 5 to 6 atoms, preferably a heterocycle with 4 to 5 carbon atoms and one oxygen atom, substituted with hydroxyl groups.
  • the fatty acids are selected advantageously from the group constituted by stearic, isostearic, linolenic, oleic, linoleic, behenic, arachidonic, ricinoleic, palmitic, myristic, lauric, and capric acids, used alone or in a mixture.
  • the fatty acids may originate from transesterification or saponification of vegetable oils and/or of animal fats.
  • the preferred vegetable oils and/or animal fats will be selected as a function of their concentration of oleic acid. Reference may be made for example to Table 6.21 of chapter 6 of the work Carburants & Moteurs [Fuels & Engines] by J. C. Guibet and E.
  • the fatty acids may also originate from fatty acids derived from tall oil (Tall Oil Fatty Acids), which comprise a majority quantity of fatty acids, typically greater than or equal to 90% by mass, as well as smaller quantities of resin acids and unsaponifiables, i.e. in quantities generally below 10%.
  • Tall Oil Fatty Acids which comprise a majority quantity of fatty acids, typically greater than or equal to 90% by mass, as well as smaller quantities of resin acids and unsaponifiables, i.e. in quantities generally below 10%.
  • the polyol will preferably be selected from the linear or branched polyols comprising more than three hydroxyl functions and the polyols comprising at least one ring of 5 or 6 atoms, preferably a heterocycle with 4 to 5 carbon atoms and one oxygen atom, optionally substituted with hydroxyl groups, used alone or in a mixture.
  • the polyol is selected from the polyols comprising at least one ring of 5 or 6 atoms, preferably a heterocycle with 4 to 5 carbon atoms and one oxygen atom, optionally substituted with hydroxyl groups, used alone or in a mixture.
  • the polyol is selected from the polyols comprising at least two heterocycles with 4 or 5 carbon atoms and one oxygen atom, linked by the formation of an acetal bond between a hydroxyl function of each ring, said heterocycles optionally being substituted with hydroxyl groups.
  • the polyol is, in particular, selected from the group consisting of erythritol, xylitol, arabitol, ribitol, sorbitol, maltitol, isomaltitol, lactitol, volemitol, mannitol, pentaerythritol, 2-hydroxymethyl-1,3-propandediol, 1,1,1-tri(hydroxymethyl)ethane, trimethylolpropane, sorbitan and the carbohydrates such as sucrose, fructose, maltose, glucose and saccharose, preferably sorbitan.
  • compound A is selected from the sorbitan partial esters, preferably the sorbitan di-, mono- and triesters, used alone or in a mixture. According to a variant, compound A is selected from the sorbitan partial esters comprising more than 40% by mass of sorbitan triesters, preferably more than 50% by mass.
  • compound A is selected from the sorbitan partial esters comprising more than 20% by mass of sorbitan monoesters and/or more than 20% by mass of sorbitan diesters, preferably more than 20% by mass of sorbitan monoesters and/or more than 30% by mass of sorbitan diesters, more preferably more than 25% by mass of sorbitan monoesters and/or more than 35% by mass of sorbitan diesters.
  • compound A is selected from the monoester(s) and/or diester(s) of polyglycerols derived from fatty acid(s), having more than 50% by number of fatty chains comprising between 12 and 24 carbon atoms.
  • polyglycerols described in document WO2013/120985, are cited by way of example and/or incorporated by reference in the present application.
  • Compound A is preferably selected from the monoester(s) and/or diester(s) of diglycerol and/or of triglycerol.
  • the partial esters of diglycerol and/or of triglycerol comprise at least 50% by mass of monoester(s) and/or of diester(s) of oleic acid and of diglycerol, thus of diglycerol mono-oleate(s) (DGMO) and/or of diglycerol dioleate(s) (DGDO), either at least 50% by mass of mono- and/or diester(s) of oleic acid and of triglycerol, or at least 50% by mass of mono- and/or diester(s) of oleic acid and of diglycerol and/or of triglycerol.
  • DGMO diglycerol mono-oleate
  • DGDO diglycerol dioleate
  • each of the first, second and third additives are constituted solely by their respective active ingredient, namely the triazole derivative in the case of the first additive, the quaternary ammonium salt in the case of the second additive and compound A in the case of the third additive.
  • the composition of additives comprises the first additive, the quaternary ammonium salt obtained from the nitrogen-containing compound (a) and a compound A selected from the sorbitan partial esters described above, preferably a sorbitan triester.
  • the composition of additives comprises the first additive, the quaternary ammonium salt obtained from the nitrogen containing compound (a) and a compound A selected from the monoesters and/or diesters of polyglycerols derived from fatty acid as described above.
  • the composition of additives comprises the first additive, the quaternary ammonium salt obtained from the nitrogen-containing compound (b) and a compound A selected from the sorbitan partial esters described above, preferably a sorbitan triester.
  • the composition of additives comprises the first additive, the quaternary ammonium salt obtained from the nitrogen-containing compound (b) and a compound A selected from the monoesters and/or diesters of polyglycerols derived from fatty acid as described above.
  • the composition of additives comprises the first additive, the quaternary ammonium salt obtained from the nitrogen-containing compound (c) and a compound A selected from the sorbitan partial esters described above, preferably a sorbitan triester.
  • the composition of additives comprises the first additive, the quaternary ammonium salt obtained from the nitrogen-containing compound (c) and a compound A selected from the monoesters and/or diesters of polyglycerols derived from fatty acid as described above.
  • composition of additives described above may also comprise one or more other conventional additives.
  • antioxidants combustion improvers, corrosion inhibitors, low temperature performance additives, dyes, demulsifiers, metal deactivators, antifoaming agents, cetane number improvers, lubricity additives, co-solvents and compatibilizing agents.
  • the other functional additive or additives may be selected from:
  • composition of additives according to the present invention may be incorporated in the fuel by any known process.
  • the composition of additives may be incorporated in the form of a concentrate comprising said composition and a solvent, compatible with the fuel, the composition being dispersed or dissolved in the solvent. Concentrates of this kind generally contain from 1 to 95%, preferably from 20 to 95% by mass of solvents.
  • the composition of additives typically comprises between 5 and 99%, preferably between 5 and 80% by mass of additives.
  • the solvents are organic solvents, which generally contain hydrocarbon solvents.
  • solvents petroleum fractions, such as naphtha, kerosene, heating oil; aliphatic and/or aromatic hydrocarbons such as hexane, pentane, decane, pentadecane, toluene, xylene, and/or ethylbenzene and the alkoxyalkanols such as 2-butoxyethanol and/or mixtures of hydrocarbons and optionally of co-solvents or compatibilizing agents, such as 2-ethylhexanol, decanol, isodecanol and/or isotridecanol may be mentioned.
  • composition of additives as described above may be used as a fuel additive.
  • the composition of additives according to the invention is particularly suitable for use in a diesel fuel having a sulphur content less than or equal to 500 ppm by mass, preferably comprising a bio diesel.
  • the diesel fuels are liquid fuels for compression engines.
  • diesel fuel is meant fuels comprising middle distillates with a boiling point between 100 and 500° C.; their wax appearance temperature WAT is often greater than or equal to ⁇ 20° C., and generally comprised between ⁇ 15° C. and +10° C.
  • distillates are mixtures of bases that may be selected for example from distillates obtained by direct distillation of petroleum or of crude hydrocarbons, vacuum distillates, hydrotreated distillates, distillates originating from catalytic cracking and/or hydrocracking of vacuum distillates, distillates resulting from conversion processes of the ARDS type (by desulphurization of atmospheric residue) and/or from visbreaking.
  • the diesel fuels according to the invention may also contain light cuts such as the gasolines originating from distillation, from catalytic or thermal cracking units, alkylation, isomerization, desulphurization units, steam cracking units.
  • the diesel fuels may contain new sources of distillates, among which the following may in particular be mentioned:
  • the diesel fuel according to the invention may also comprise or be solely constituted by one or more biofuels.
  • biofuel is meant the fuels obtained from organic matter (biomass), in contrast to the fuels originating from fossil resources.
  • bio diesels also called biodiesels
  • alcohols may be mentioned.
  • the alcohols such as methanol, ethanol, butanols, ethers (MTBE, ETBE, etc.) are generally used in a mixture with gasoline fuels, but sometimes with heavier fuels of the diesel type.
  • Biodiesel or bio gas oil is an alternative to the standard fuel for diesel engines.
  • This biofuel is obtained from vegetable or animal oil (including used cooking oils) transformed by a chemical process called transesterification, causing this oil to react with an alcohol in order to obtain fatty acid esters.
  • transesterification a chemical process called transesterification
  • fatty acid methyl esters FAME
  • FAEE fatty acid ethyl esters
  • the Vegetable Oil or Fatty Acid Methyl or Ethyl Esters (VOME, VOEE, FAME, FAEE) may be mentioned; for the vegetable and/or animal oils, the hydrotreated and/or hydrocracked and/or hydrodeoxygenated (HDO) vegetable and/or animal oils may be mentioned.
  • Mixtures of middle distillates of fossil origin and of bio diesel are generally denoted by the letter “B” followed by a number indicating the percentage of bio diesel contained in the diesel.
  • B99 contains 99% of bio diesel and 1% of middle distillates of fossil origin; B20, 20% of bio diesel and 80% of middle distillates of fossil origin etc.
  • diesel fuels of type B0 which do not contain oxygenated compounds
  • bio diesel of type Bx which contain x % (v/v) of vegetable oil or fatty acid esters, most often methyl esters (VOME or FAME).
  • VOME methyl esters
  • diesel fuel preferably has a sulphur content less than or equal to 500 ppm by mass, advantageously less than or equal to 100 ppm by mass, and may reach a content less than or equal to 50 ppm by mass, or even less than or equal to 10 ppm by mass (this is case for current diesel fuels for vehicles, the sulphur content of which according to European standard EN 590 currently in force must be less than or equal to 10 ppm by mass).
  • the diesel fuel advantageously comprises up to 30% by volume of bio diesel, preferably up to 20% by volume, more preferably up to 10% by volume.
  • the composition of additives is preferably incorporated in the fuel so as to obtain a concentration by mass of each additive contained in said composition in the range from 5 to 5000 ppm, preferably from 20 to 500 ppm, more preferably from 30 to 250 ppm in the fuel.
  • the concentration by mass is calculated relative to the total mass of the fuel.
  • the concentration by mass of each first and second additive and optionally third additive varies from 5 to 5000 ppm, and preferably between 20 and 500 ppm, more preferably between 30 and 250 ppm.
  • a person skilled in the art will easily adapt the concentration of the composition of additives according to the invention as a function of optional dilution of the additives in a solvent, to obtain the desired concentration of each functional additive in the final fuel.
  • the fuel preferably comprises at least 5 ppm by mass, preferably at least 100 ppm by mass of the composition of additives according to the invention. It will be possible for up to 10% by mass, preferably up to 1% by mass, more preferably up to 0.5% by mass of additives, including the composition of additives, to be incorporated in a fuel.
  • the mass ratio of the first to the second additive (first:second) is between 1:100 and 100:1, preferably between 1:10 and 10:1, even more preferably between 1:2 and 2:1.
  • the mass ratio of the second to the third additive (second:third) is between 1:100 and 1:1, preferably between 1:10 and 1:1, even more preferably between 1:5 and 1:1.
  • the diesel fuel described above may be used in a diesel engine, to improve the performance of said engine, in particular to limit the deposits in said engine, preferably in a direct-injection engine, more preferably when the engine is equipped with a high-pressure injection system (“common-rail”).
  • Use of such a fuel incorporating the composition of additives according to the present invention makes it possible to reduce the fuel consumption of the diesel engine (“Fuel Eco” effect), and in particular makes it possible to minimize the loss of power of said engine.
  • the present invention also relates to a process for maintaining the cleanliness of a diesel engine (“keep-clean” effect) by limiting the deposits of soap and/or lacquer in the internal components of the injection systems of said engine and/or for cleaning the fouled internal parts of the injection system of said engine, by removing, at least partly, the deposits of soap and/or lacquer in said internal parts (curative “clean-up” effect).
  • Said process comprises the combustion of a composition of additives according to the present invention in a diesel engine, in particular in a direct-injection engine, preferably with a high-pressure injection system (“common-rail”).
  • a 500 mL flask is loaded with 100 g of polyisobutenyl succinic anhydride (PIBSA) with 84% of active ingredient (76.64 mmol), and 26.3 g of an aromatic solvent of the brand “Solvesso 150ND” is added.
  • PIBSA polyisobutenyl succinic anhydride
  • an aromatic solvent of the brand “Solvesso 150ND” is added.
  • the reaction medium is heated to 140° C., under vigorous stirring, and then 5.15 g (0.8 eq./61.31 mmol) of 3-amino-1,2,4-triazole is introduced. It is then heated under reflux for 4 h in order to remove 1.10 mL of water in the Dean Stark.
  • PIBSA polyisobutenyl succinic anhydride
  • DMAP dimethylaminopropylamine
  • Protocol 1 Evaluation of the “Lacquering” Resistance for the Deposits of the IDID Type
  • the technology used for the injectors requires a high fuel return, which promotes degradation of the fuel since it may be subjected to several cycles in the pump and high-pressure chamber before being injected into the combustion chamber.
  • a variant of the method for testing the clean-up effect i.e. cleaning of the type 1 and/or type 2 deposits has also been developed. It is based on the preceding method but is separated into two parts of 40 h and then 30 h:
  • the injectors are dismantled at the end of the test to examine and assess the deposits formed along the needles.
  • the procedure adopted for assessing the needles is as follows:
  • the scale of the scores varies from ⁇ 1 (in the case of a very fine soap) to ⁇ 10 (in the case of a very thick, strongly coloured soap).
  • a value of the effect of the soap is determined by calculating the arithmetic mean of the scores obtained on the population of points of the needle assessed.
  • the scale of the scores varies from 1 (in the case of a black lacquer equivalent to significant deposition of lacquer) to 10 (in the case of a very clear lacquer equivalent to a new needle).
  • a value of the effect of the lacquer is calculated by finding the sum of the number of points belonging to the score (1 to 10) divided by the value of the score.
  • An overall score (N) out of 10 is then determined by weighting the effect of the lacquers and soaps.
  • Protocol 2 Measurement of Loss of Power in a Diesel Engine with a High-Pressure Injection System (DW10+Zn)
  • the fuel is tested in a Peugeot DW10 engine using injectors complying with the Euro 5 standards according to the process CEC F-98-8 DW10BTED4 developed and published by the Coordinating European Council (CEC).
  • CEC Coordinating European Council
  • a small quantity of zinc neodecanoate (1 ppm) is added to the test fuel. This test was developed for distinguishing between fuels based on their capacity for producing or avoiding external deposits of the injection system relating to coking or clogging of the injection nozzles (nozzle coking or fouling).
  • This test allows fuels to be differentiated on the basis of the loss of power caused by the deposits of the coking type (comparison between the percentage loss of power).
  • This test in particular makes it possible to differentiate a fuel that produces little deposition of the coking type (loss of power ⁇ 2%) from those that produce sufficient coking to cause a loss of power of 2% or more, regarded as unacceptable for the engine manufacturers.
  • B7 diesel manufactured in France containing 7% of FAME (fatty acid methyl ester) and complying with EN 590).
  • the test on the fuel to be evaluated then takes a total of 44 hours, not counting the periods for preparation and cooling.
  • the time of 44 hours is divided into 32 hours of engine operation and 12 hours with the engine stopped.
  • Air temperature Time Speed Load Torque after exchanger Step (min) (rpm) (%) (Nm) (° C.) 1 2 1750 20 62 45 2 7 3000 60 173 50 3 2 1750 20 62 45 4 7 3000 80 212 50 5 2 1750 20 62 45 6 10 4000 100 * 50 7 2 1250 (10) 20 43 8 7 3000 100 * 50 9 2 1250 (10) 20 43 10 10 2000 100 * 50 11 2 1250 (10) 20 43 12 7 4000 100 * 50
  • the engine speed is adjusted to 1000 rpm/10 Nm in 60 s and is maintained at this speed for 300 s.
  • the overall cycle 1 to 4 is repeated 4 times.
  • the loss of power is measured in each operating cycle, i.e. 32 in total.
  • Test 1 Resistance to “Lacquering”
  • tests G, G′ and G′′ correspond to the same test, G corresponding to the result for the batch of injectors 1 , G′ corresponding to the result for the batch of injectors 2 and G′′ corresponding to the result for the batch of injectors 3 .
  • Test G corresponds to the fouling phase (“Dirty-up”), test G′ to the cleaning phase (“Clean-up”) and test G′′ to the phase of maintenance of cleanliness (“keep-clean”).
  • fuel 4 containing a combination of the first, second and third additives has both a preventive (Keep-clean) and curative (Clean-up) effect.
  • fuel 5 containing a triazole derivative not covered by the present invention does not have a significant curative effect (Clean-up).
  • the quantities shown in Table 5 are quantities by mass (mg/kg).
  • the fuels containing the composition of additives according to the present invention are particularly remarkable in that they do not generate deposits of the coking type compared with a fuel containing a quaternary ammonium salt alone (fuel 7) or a combination of a quaternary ammonium salt and a triazole derivative different from those covered by the present invention (fuels 8 and 9).
  • a triazole derivative according to the invention in combination with a quaternary ammonium salt and optionally a compound A as described above confers upon the fuel both control of deposits of the lacquering type (IDID deposit) and/or resistance to deposits of the coking type.
  • composition of additives according to the present invention is remarkable in that it makes it possible to obtain fuels having improved performance, in particular in the case of diesel fuels with a low sulphur content, optionally containing a bio diesel.
  • the particular combination of additives described above in particular makes it possible to reduce the fuel consumption of diesel engines, by combining a clean-up effect and keep-clean effect, minimizing the loss of power and improving the wear resistance of said fuel.

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FR3071850B1 (fr) 2017-10-02 2020-06-12 Total Marketing Services Composition d’additifs pour carburant
BR112020009528A2 (pt) * 2017-11-17 2020-11-03 Dorf Ketal Chemicals Fze composições de aditivos de combustível e seus métodos de uso
GB201805238D0 (en) * 2018-03-29 2018-05-16 Innospec Ltd Composition, method and use
KR101950489B1 (ko) * 2018-07-11 2019-02-20 주식회사 동이기술 자동차 연료 첨가제 조성물
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WO2020109568A1 (en) 2018-11-30 2020-06-04 Total Marketing Services Quaternary fatty amidoamine compound for use as an additive for fuel
FR3092334B1 (fr) * 2019-01-31 2022-06-17 Total Marketing Services Utilisation d’une composition de carburant à base d’hydrocarbures paraffiniques pour nettoyer les parties internes des moteurs diesels
FR3092333B1 (fr) 2019-01-31 2021-01-08 Total Marketing Services Composition de carburant à base d’hydrocarbures paraffiniques
FR3103812B1 (fr) 2019-11-29 2023-04-07 Total Marketing Services Utilisation de composés alkyl phénol comme additifs de détergence
FR3103815B1 (fr) 2019-11-29 2021-12-17 Total Marketing Services Utilisation de diols comme additifs de détergence
FR3110913B1 (fr) * 2020-05-29 2023-12-22 Total Marketing Services Composition d’additifs pour carburant moteur
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